Canonical Allele Identifier: CA057001

Gene: APOB

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21022971C>T , CM000664.2:g.21022971C>T	GRCh38
NC_000002.11:g.21245843C>T , CM000664.1:g.21245843C>T	GRCh37
NC_000002.10:g.21099348C>T	NCBI36
NG_011793.1:g.26103G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1982G>A	ENSP00000501110.2:n.*1982G>A
ENST00000673882.2:c.*1982G>A	ENSP00000501253.2:n.*1982G>A
ENST00000673739.1:c.2390G>A	ENSP00000501110.1:n.2390G>A
ENST00000673882.1:c.2390G>A	ENSP00000501253.1:n.2390G>A
ENST00000233242.5:c.2676G>A MANE Select	ENSP00000233242.1:p.Pro892=
ENST00000616098.4:c.2676G>A	ENSP00000477990.1:p.Pro892=
NM_000384.2:c.2676G>A	NP_000375.2:p.Pro892=
XM_011532809.1:c.2676G>A	XP_011531111.1:p.Pro892=
NM_000384.3:c.2676G>A MANE Select	NP_000375.3:p.Pro892=